State Key Laboratory of Medical Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Shanghai Key Laboratory of Hypertension, Shanghai Institute of Hypertension, Shanghai, China.
Division of Cardiology, Department of Medicine, University of Alberta, Edmonton, Canada; Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Canada; Department of Physiology, University of Alberta, Edmonton, Canada.
Biochim Biophys Acta Mol Basis Dis. 2017 Aug;1863(8):1942-1950. doi: 10.1016/j.bbadis.2016.11.007. Epub 2016 Nov 4.
The apelin/apelin receptor system is widely distributed and has a dominant role in cardiovascular homeostasis and disease. The apelin gene is X-linked and is synthesized as a 77 amino acid pre-pro-peptide that is subsequently cleaved to generate a family of apelin peptides that possess similar functions but display different tissue distribution, potency and receptor binding affinity. Loss-of-function experiments using the apelin and the apelin receptor knockout mice and gain-of-function experiments using apelin peptides have delineated a well-defined role of the apelin axis in cardiovascular physiology and diseases. Activation of the apelin receptor by its cognate peptide ligand, apelin, induces a wide range of physiological effects, including vasodilation, increased myocardial contractility, angiogenesis, and balanced energy metabolism and fluid homeostasis. The apelin/apelin receptor pathway is also implicated in atherosclerosis, hypertension, coronary artery disease, heart failure, diabetes and obesity, making it a promising therapeutic target. Hence, research is expanding to develop novel therapies that inhibit degradation of endogenous apelin peptides or their analogues. Chemical synthesis of stable apelin receptor agonists aims to more efficiently enhance the activation of the apelin system. Targeting the apelin/apelin receptor axis has emerged as a novel therapeutic approach against cardiovascular diseases and an increased understanding of cardiovascular actions of the apelin system will help to develop effective interventions.
Apelin/APJ 系统广泛分布,在心血管稳态和疾病中起主要作用。Apelin 基因位于 X 染色体上,合成的前体肽由 77 个氨基酸组成,随后被切割生成具有相似功能但组织分布、效力和受体结合亲和力不同的一系列 Apelin 肽。使用 Apelin 和 Apelin 受体敲除小鼠的功能丧失实验以及使用 Apelin 肽的功能获得实验,明确了 Apelin 轴在心血管生理学和疾病中的作用。其同源肽配体 Apelin 激活 Apelin 受体,诱导广泛的生理效应,包括血管舒张、心肌收缩力增加、血管生成以及平衡的能量代谢和液体稳态。Apelin/APJ 途径还与动脉粥样硬化、高血压、冠心病、心力衰竭、糖尿病和肥胖有关,使其成为有前途的治疗靶点。因此,研究正在扩展,以开发抑制内源性 Apelin 肽或其类似物降解的新型疗法。稳定的 Apelin 受体激动剂的化学合成旨在更有效地增强 Apelin 系统的激活。针对 Apelin/APJ 轴已成为治疗心血管疾病的新方法,对 Apelin 系统心血管作用的深入了解将有助于开发有效的干预措施。